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Hornerin deposits in neuronal intranuclear inclusion disease: direct identification of proteins with compositionally biased regions in inclusions.
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- Acta Neuropathologica Communications, 2022, v. 10, n. 1, p. 1, doi. 10.1186/s40478-022-01333-8
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- Publication type:
- Article
Proteomic analysis of heat-stable proteins revealed an increased proportion of proteins with compositionally biased regions.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-08044-z
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- Article
Semi-rational engineering of a coral fluorescent protein into an efficient highlighter.
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- EMBO Reports, 2005, v. 6, n. 3, p. 233, doi. 10.1038/sj.embor.7400361
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- Publication type:
- Article
Intracellular localization and splicing regulation of FUS/TLS are variably affected by amyotrophic lateral sclerosis-linked mutations.
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- Nucleic Acids Research, 2011, v. 39, n. 7, p. 2781, doi. 10.1093/nar/gkq1162
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- Publication type:
- Article
MBNL and CELF proteins regulate alternative splicing of the skeletal muscle chloride channel CLCN1.
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- Nucleic Acids Research, 2009, v. 37, n. 19, p. 6477, doi. 10.1093/nar/gkp681
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- Article
ER Dynamics and Derangement in Neurological Diseases.
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- Frontiers in Neuroscience, 2018, p. 1, doi. 10.3389/fnins.2018.00091
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- Article
Harnessing chaperone-mediated autophagy for the selective degradation of mutant huntingtin protein.
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- Nature Biotechnology, 2010, v. 28, n. 3, p. 256, doi. 10.1038/nbt.1608
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- Publication type:
- Article
Trehalose alleviates polyglutamine-mediated pathology in a mouse model of Huntington disease.
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- Nature Medicine, 2004, v. 10, n. 2, p. 148, doi. 10.1038/nm985
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- Publication type:
- Article
Reappraisal of VAChT-Cre: Preference in slow motor neurons innervating type I or IIa muscle fibers.
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- Genesis: The Journal of Genetics & Development, 2016, v. 54, n. 11, p. 568, doi. 10.1002/dvg.22979
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- Article
Mutant VAPB: Culprit or Innocent Bystander of Amyotrophic Lateral Sclerosis?
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- Contact (25152564), 2021, p. 1, doi. 10.1177/25152564211022515
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- Publication type:
- Article
Mutant VAPB: Culprit or Innocent Bystander of Amyotrophic Lateral Sclerosis?
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- Contact (25152564), 2021, p. 1, doi. 10.1177/25152564211022515
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- Publication type:
- Article
Mutant VAPB: Culprit or Innocent Bystander of Amyotrophic Lateral Sclerosis?
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- Contact (25152564), 2021, v. 4, p. 1, doi. 10.1177/25152564211022515
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- Publication type:
- Article
FUS/TLS deficiency causes behavioral and pathological abnormalities distinct from amyotrophic lateral sclerosis.
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- Acta Neuropathologica Communications, 2015, v. 3, n. 1, p. 1, doi. 10.1186/s40478-015-0202-6
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- Publication type:
- Article
Acidic mammalian chitinase is a proteases-resistant glycosidase in mouse digestive system.
- Published in:
- Scientific Reports, 2016, p. 37756, doi. 10.1038/srep37756
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- Publication type:
- Article
FUS/TLS acts as an aggregation-dependent modifier of polyglutamine disease model mice.
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- Scientific Reports, 2016, p. 35236, doi. 10.1038/srep35236
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- Publication type:
- Article
Differential roles of NF-Y transcription factor in ER chaperone expression and neuronal maintenance in the CNS.
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- Scientific Reports, 2016, p. 34575, doi. 10.1038/srep34575
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- Publication type:
- Article
Structure-based site-directed photo-crosslinking analyses of multimeric cell-adhesive interactions of voltage-gated sodium channel β subunits.
- Published in:
- Scientific Reports, 2016, p. 26618, doi. 10.1038/srep26618
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- Publication type:
- Article
Large-Scale RNA Interference Screening in Mammalian Cells Identifies Novel Regulators of Mutant Huntingtin Aggregation.
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- PLoS ONE, 2014, v. 9, n. 4, p. 1, doi. 10.1371/journal.pone.0093891
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- Publication type:
- Article
Loss of aPKCλ in Differentiated Neurons Disrupts the Polarity Complex but Does Not Induce Obvious Neuronal Loss or Disorientation in Mouse Brains.
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- PLoS ONE, 2013, v. 8, n. 12, p. 1, doi. 10.1371/journal.pone.0084036
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- Publication type:
- Article
RNAi Screening in Drosophila Cells Identifies New Modifiers of Mutant Huntingtin Aggregation.
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- PLoS ONE, 2009, v. 4, n. 9, p. 1, doi. 10.1371/journal.pone.0007275
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- Publication type:
- Article
A novel therapeutic strategy for polyglutamine diseases by stabilizing aggregation-prone proteins with small molecules.
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- Journal of Molecular Medicine, 2005, v. 83, n. 5, p. 343, doi. 10.1007/s00109-004-0632-2
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- Publication type:
- Article
Generation and characterization of cerebellar granule neurons specific knockout mice of Golli-MBP.
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- Transgenic Research, 2024, v. 33, n. 3, p. 99, doi. 10.1007/s11248-024-00382-0
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- Publication type:
- Article
Rapid dissemination of alpha-synuclein seeds through neural circuits in an in-vivo prion-like seeding experiment.
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- Acta Neuropathologica Communications, 2018, v. 6, n. 1, p. N.PAG, doi. 10.1186/s40478-018-0587-0
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- Publication type:
- Article
A Functional Null Mutation of SCN1B in a Patient with Dravet Syndrome.
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- Journal of Neuroscience, 2009, v. 29, n. 34, p. 10764, doi. 10.1523/JNEUROSCI.2475-09.2009
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- Publication type:
- Article
Cross-Seeding Fibrillation of Q/N-Rich Proteins Offers New Pathomechanism of Polyglutamine Diseases.
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- Journal of Neuroscience, 2009, v. 29, n. 16, p. 5153, doi. 10.1523/JNEUROSCI.0783-09.2009
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- Publication type:
- Article
Deranged Calcium Signaling and Neurodegeneration in Spinocerebellar Ataxia Type 3.
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- Journal of Neuroscience, 2008, v. 28, n. 48, p. 12713, doi. 10.1523/JNEUROSCI.3909-08.2008
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- Publication type:
- Article
Suppression of Mutant Huntingtin Aggregate Formation by Cdk5/p35 through the Effect on Microtubule Stability.
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- Journal of Neuroscience, 2008, v. 28, n. 35, p. 8747, doi. 10.1523/JNEUROSCI.0973-08.2008
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- Publication type:
- Article
Mutant Huntingtin reduces HSP70 expression through the sequestration of NF-Y transcription factor.
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- EMBO Journal, 2008, v. 27, n. 6, p. 827, doi. 10.1038/emboj.2008.23
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- Publication type:
- Article
Proteomics-Based Approach Identifies Altered ER Domain Properties by ALS-Linked VAPB Mutation.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-64517-z
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- Publication type:
- Article
Cortical dysgenesis in a patient with Turner mosaicism.
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- 1996
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- Publication type:
- journal article
Genome-wide analyses in neuronal cells reveal that upstream transcription factors regulate lysosomal gene expression.
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- FEBS Journal, 2016, v. 283, n. 6, p. 1077, doi. 10.1111/febs.13650
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- Article
Aggregation of scaffolding protein DISC1 dysregulates phosphodiesterase 4 in Huntington's disease.
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- 2017
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- Publication type:
- journal article
Multiple system degeneration with basophilic inclusions in Japanese ALS patients with FUS mutation.
- Published in:
- Acta Neuropathologica, 2010, v. 119, n. 3, p. 355, doi. 10.1007/s00401-009-0621-1
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- Publication type:
- Article
Immunohistochemical study of kuru plaques using antibodies against synthetic prion protein peptides.
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- Acta Neuropathologica, 1992, v. 83, n. 6, p. 613, doi. 10.1007/BF00299410
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- Publication type:
- Article
NF-Y inactivation causes atypical neurodegeneration characterized by ubiquitin and p62 accumulation and endoplasmic reticulum disorganization.
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- Nature Communications, 2014, v. 5, n. 2, p. 3354, doi. 10.1038/ncomms4354
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- Publication type:
- Article
Sodium channel β1 subunit localizes to axon initial segments of excitatory and inhibitory neurons and shows regional heterogeneity in mouse brain.
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- Journal of Comparative Neurology, 2015, v. 523, n. 5, p. 814, doi. 10.1002/cne.23715
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- Article
The pathogenic mechanisms of polyglutamine diseases and current therapeutic strategies.
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- Journal of Neurochemistry, 2009, v. 110, n. 6, p. 1737, doi. 10.1111/j.1471-4159.2009.06302.x
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- Publication type:
- Article
Membrane microdomain switching: a regulatory mechanism of amyloid precursor protein processing.
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- Journal of Cell Biology, 2008, v. 183, n. 2, p. 339, doi. 10.1083/jcb.200804075
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- Publication type:
- Article
Gene expression profiling in neuronal cells identifies a different type of transcriptome modulated by NF-Y.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-78682-8
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- Publication type:
- Article
TBK1 controls autophagosomal engulfment of polyubiquitinated mitochondria through p62/SQSTM1 phosphorylation.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 15, p. 4429, doi. 10.1093/hmg/ddv179
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- Publication type:
- Article
Depletion of p62 reduces nuclear inclusions and paradoxically ameliorates disease phenotypes in Huntington’s model mice.
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- Human Molecular Genetics, 2015, v. 24, n. 4, p. 1092, doi. 10.1093/hmg/ddu522
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- Publication type:
- Article
Nuclear localization of MBNL1: splicing-mediated autoregulation and repression of repeat-derived aberrant proteins.
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- Human Molecular Genetics, 2015, v. 24, n. 3, p. 740, doi. 10.1093/hmg/ddu492
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- Publication type:
- Article
Dexamethasone induces heat shock response and slows down disease progression in mouse and fly models of Huntington's disease.
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- Human Molecular Genetics, 2014, v. 23, n. 10, p. 2737, doi. 10.1093/hmg/ddt667
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- Publication type:
- Article
Chromogranin-mediated secretion of mutant superoxide dismutase proteins linked to amyotrophic lateral sclerosis.
- Published in:
- Nature Neuroscience, 2006, v. 9, n. 1, p. 108, doi. 10.1038/nn1603
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- Publication type:
- Article
Intracellular seeded aggregation of mutant Cu,Zn-superoxide dismutase associated with amyotrophic lateral sclerosis.
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- FEBS Letters, 2013, v. 587, n. 16, p. 2500, doi. 10.1016/j.febslet.2013.06.046
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- Publication type:
- Article
ROCK-phosphorylated vimentin modifies mutant huntingtin aggregation via sequestration of IRBIT.
- Published in:
- Molecular Neurodegeneration, 2012, v. 7, n. 1, p. 43, doi. 10.1186/1750-1326-7-43
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- Publication type:
- Article
The Parkinson’s Disease-Associated Protein Kinase LRRK2 Modulates Notch Signaling through the Endosomal Pathway.
- Published in:
- PLoS Genetics, 2015, v. 11, n. 9, p. 1, doi. 10.1371/journal.pgen.1005503
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- Publication type:
- Article
Phosphorylation of Mitochondrial Polyubiquitin by PINK1 Promotes Parkin Mitochondrial Tethering.
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- PLoS Genetics, 2014, v. 10, n. 12, p. 1, doi. 10.1371/journal.pgen.1004861
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- Publication type:
- Article
Mutant huntingtin fragment selectively suppresses Brn-2 POU domain transcription factor to mediate hypothalamic cell dysfunction.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 11, p. 2099, doi. 10.1093/hmg/ddq087
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- Publication type:
- Article
Knock-down of PQBP1 impairs anxiety-related cognition in mouse.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 22, p. 4239, doi. 10.1093/hmg/ddp378
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- Publication type:
- Article